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基于代谢组学和脂质组学揭示消渴饮水提取物组合对高蔗糖/高脂肪饮食诱导的糖尿病小鼠的降血糖和降血脂机制。

Revealing hypoglycemic and hypolipidemic mechanism of Xiaokeyinshui extract combination on streptozotocin-induced diabetic mice in high sucrose/high fat diet by metabolomics and lipidomics.

机构信息

Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, College of Pharmacy, Huazhong University of Science and Technology, Hangkong Road 13, Wuhan, 430030, Hubei Province, China.

Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, College of Pharmacy, Huazhong University of Science and Technology, Hangkong Road 13, Wuhan, 430030, Hubei Province, China.

出版信息

Biomed Pharmacother. 2021 Mar;135:111219. doi: 10.1016/j.biopha.2021.111219. Epub 2021 Feb 1.

DOI:10.1016/j.biopha.2021.111219
PMID:33433360
Abstract

Type 2 diabetic mellitus (T2DM), often accompanied by disorders of glucose and lipid metabolism, has troubled hundreds of millions of people. Xiaokeyinshui extract combination (XEC), derived from traditional Chinese medicines formula, has exerted hypoglycemic effects against T2DM. However, its mechanism of metabolic level is still unclear. In this study, a T2DM mice model, induced by a high sucrose/high fat diet combined with low-dose streptozotocin (STZ) injections, was adopted. The biochemical index was determined and a combination of metabolomics and lipidomics analyses of plasma were performed. The results showed that XEC increased secretion of insulin and level of HDL-C, decreased levels of FBG, HbA1c, TC, TG, LDL-C and repaired islet structure in diabetic mice. In addition, the metabolic profiles of plasma were analyzed and 54 potential biomarkers were screened out, mainly including carbohydrates, lipids and amino acids. These potential biomarkers were found to be correlated with the following pathways: galactose metabolism, fructose and mannose metabolism, TCA cycle, arachidonic acid metabolism, glycerolipid metabolism, glycerophospholipid metabolism, sphingolipid metabolism and amino acid metabolism. In conclusion, we speculated that carbohydrate metabolism, lipid metabolism and amino acid metabolism played roles in the therapeutic mechanisms of XEC on T2DM.

摘要

2 型糖尿病(T2DM)常伴有糖、脂代谢紊乱,困扰着数以亿计的人群。消渴饮水提取物组合(XEC)来源于中药方剂,对 T2DM 具有降糖作用。但其代谢水平的机制尚不清楚。本研究采用高蔗糖/高脂肪饮食联合小剂量链脲佐菌素(STZ)注射诱导 T2DM 小鼠模型,测定生化指标,进行血浆代谢组学和脂质组学分析。结果表明,XEC 能增加糖尿病小鼠胰岛素分泌和高密度脂蛋白胆固醇(HDL-C)水平,降低空腹血糖(FBG)、糖化血红蛋白(HbA1c)、总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)水平,修复胰岛结构。此外,对血浆代谢谱进行分析,筛选出 54 个潜在生物标志物,主要涉及碳水化合物、脂质和氨基酸。这些潜在的生物标志物与以下途径有关:半乳糖代谢、果糖和甘露糖代谢、三羧酸循环、花生四烯酸代谢、甘油酯代谢、甘油磷脂代谢、鞘脂代谢和氨基酸代谢。总之,我们推测 XEC 治疗 T2DM 的作用机制与碳水化合物代谢、脂质代谢和氨基酸代谢有关。

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